Canonical Allele Identifier: CA2693446483

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675576-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675576C>A , CM000685.2:g.38675576C>A	GRCh38
NC_000023.10:g.38534830C>A , CM000685.1:g.38534830C>A	GRCh37
NC_000023.9:g.38419774C>A	NCBI36
NG_009160.1:g.119100C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-129C>A MANE Select	ENSP00000367743.2:n.442-129C>A
ENST00000286824.6:c.493-129C>A	ENSP00000286824.6:n.493-129C>A
ENST00000378482.6:c.442-129C>A	ENSP00000367743.2:n.442-129C>A
ENST00000419600.3:n.386-129C>A
ENST00000465127.1:c.532-129C>A	ENSP00000417050.1:n.532-129C>A
ENST00000471410.5:c.*468-129C>A	ENSP00000419290.1:n.*468-129C>A
ENST00000475216.5:c.*435-129C>A	ENSP00000418586.1:n.*435-129C>A
ENST00000488893.5:n.625-129C>A
NM_004615.3:c.442-129C>A	NP_004606.2:n.442-129C>A
NM_004615.4:c.442-129C>A MANE Select	NP_004606.2:n.442-129C>A